Canonical Allele Identifier: PA2579795928
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ser19Ala
CA410602537
NM_000071.3:c.55T>G
CA2579804658
NM_000071.3:c.55_57delinsGCG
CA2579804661
NM_000071.3:c.55_57delinsGCC
CA2579804664
NM_000071.3:c.55_57delinsGCT